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WECK IPN914973Recalls & reported problems

Teleflex Incorporated · Class 1

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 24026704710137), received between Jul 29, 2021 and Jul 29, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Activation, Positioning or Separation Problem” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Activation, Positioning or Separation Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJul 29, 2021Activation, Positioning or Separation Problem; Activation, Positioning or Separation Problem

    ALLEGED ISSUE: INFORMALLY IN SURGERY ROOMS THEY INFORM ME THAT THE CLIPS DID NOT CLOSE SINCE THE CLAMP WAS NOT IN GOOD CONDITION. THE CLIPS HAVE BEEN USED WITHOUT ANY PROBLEM WITH OTHER CLAMPS. I HAVE NOT RECEIVED A FORMAL QUALITY REPORT FROM THE INSTITUTION. THE CLAMP WAS REMOVED AND THE APPLIER IS AVAILABLE TO BE SHIPPED PHYSICALLY. MEDICAL INTERVENTION WAS NECESSARY BUT PATIENT IS FINE, NO PATIENT HARMED WAS REPORTED. I DO NOT HAVE MORE DETAILS, THE CLIENT DOES NOT HAVE ADDITIONAL INFORMATION.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12245102 ↗

Other Applier, surgical, clip devices

All Applier, surgical, clip devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.